EP3307802A1 - Fleckenbeständige soft-touch-beschichtungszusammensetzungen und daraus hergestellte beschichtungen - Google Patents

Fleckenbeständige soft-touch-beschichtungszusammensetzungen und daraus hergestellte beschichtungen

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Publication number
EP3307802A1
EP3307802A1 EP16732824.4A EP16732824A EP3307802A1 EP 3307802 A1 EP3307802 A1 EP 3307802A1 EP 16732824 A EP16732824 A EP 16732824A EP 3307802 A1 EP3307802 A1 EP 3307802A1
Authority
EP
European Patent Office
Prior art keywords
coating composition
polyester polyol
weight
coating
fluoropolymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP16732824.4A
Other languages
English (en)
French (fr)
Other versions
EP3307802B1 (de
EP3307802B2 (de
Inventor
Gereme Thomas HENSEL
Renlong Gao
Irina G. Schwendeman
Gobinda Saha
Jiping Shao
Courtney RICHMAN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
PPG Industries Ohio Inc
Original Assignee
PPG Industries Ohio Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=56264054&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP3307802(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by PPG Industries Ohio Inc filed Critical PPG Industries Ohio Inc
Priority to PL16732824T priority Critical patent/PL3307802T3/pl
Publication of EP3307802A1 publication Critical patent/EP3307802A1/de
Publication of EP3307802B1 publication Critical patent/EP3307802B1/de
Application granted granted Critical
Publication of EP3307802B2 publication Critical patent/EP3307802B2/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C09D175/06—Polyurethanes from polyesters
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4018—Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4063—Mixtures of compounds of group C08G18/62 with other macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
    • C08G18/423—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing cycloaliphatic groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
    • C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
    • C08G18/4241—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols from dicarboxylic acids and dialcohols in combination with polycarboxylic acids and/or polyhydroxy compounds which are at least trifunctional
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/46—Polycondensates having carboxylic or carbonic ester groups in the main chain having heteroatoms other than oxygen
    • C08G18/4607—Polycondensates having carboxylic or carbonic ester groups in the main chain having heteroatoms other than oxygen having halogens
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/50—Polyethers having heteroatoms other than oxygen
    • C08G18/5003—Polyethers having heteroatoms other than oxygen having halogens
    • C08G18/5015—Polyethers having heteroatoms other than oxygen having halogens having fluorine atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/58—Epoxy resins
    • C08G18/582—Epoxy resins having halogens
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6275—Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6279—Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds containing fluorine atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds
    • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/181—Acids containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes

Definitions

  • the present invention relates to coating compositions that can provide good stain resistance and soft touch properties, coatings formed from these coating compositions, and substrates at least partially coated with such coatings.
  • Coatings applied to consumer electronic devices such as cellular phones, portable notebooks, laptops, and the like are often designed to have a soft touch or feel.
  • these soft touch coatings often exhibit poor stain resistance.
  • most soft touch coatings are typically restricted to application on black or other dark substrates.
  • Various attempts have been made to improve the stain resistance of soft touch coatings to expand their application to white and other light colored substrates.
  • improvement of stain resistance is often accompanied by a deterioration of the soft touch properties.
  • the present invention is directed to a coating composition that includes: (a) a fluoropolymer comprising at least one reactive functional group; (b) a polyester polyol; and (c) a crosslinker reactive with (a) and (b).
  • the polyester polyol includes a reaction product obtained from a mixture of reactants including: an aliphatic diol; a polyol having 3 or more hydroxyl groups; and a cyclic polycarboxylic acid, or an anhydride or ester thereof.
  • the present invention also includes substrates, electronic products, and electronic components at least partially coated with the coating compositions described herein. DESCRIPTION OF THE INVENTION
  • any numerical range recited herein is intended to include all sub-ranges subsumed therein.
  • a range of "1 to 10" is intended to include all sub-ranges between (and including) the recited minimum value of 1 and the recited maximum value of 10, that is, having a minimum value equal to or greater than 1 and a maximum value of equal to or less than 10.
  • the present invention is directed to a coating composition that includes a fluoropolymer having at least one reactive functional group.
  • a fluoropolymer refers to a polymer derived from one or more monomers with at least one of the monomers having at least one pendant fluorine substituent.
  • the fluoropolymer can include a polymer that has a monomelic repeat unit selected from chlorotrifluoroethylene, tetrafluoroethylene, perfluoro(methyl vinyl ether), perfluoro(propyl vinyl ether), perfluoro(ethyl vinyl ether), vinylidene fluoride, hexafluoropropylene, and combinations thereof.
  • the fluoropolymer can also include a polymer that has a monomelic repeat unit selected from tetrafluoroethylene oxide, hexafluoropropylene oxide, and combinations thereof.
  • polymer refers to oligomers and homopolymers (e.g., prepared from a single monomer species), copolymers (e.g., prepared from at least two monomer species), and graft polymers.
  • the term “resin” is used interchangeably with “polymer.”
  • the fluoropolymer and other resins such a polyester polyol described herein can be used to form a film.
  • a "film-forming resin” refers to resins that can form a self-supporting continuous film on at least a horizontal surface of a substrate upon removal of any diluents or carriers present in the composition.
  • Non-limiting examples of suitable fluoropolymers that can be used with the coating compositions of the present invention include fluoroethylene/alkyl vinyl ether copolymer, perfluoropolyether, a chlorotrifluoroethylene copolymer, polyvinylidene fluoride, a tetrafluoroethylene copolymer, polyhexafluoropropylene, polytetrafluoroethylene, and combinations thereof and which comprise or are modified to comprise at least one reactive functional group.
  • Suitable fluoropolymers are also commercially available from Asahi Glass Co. under the trade name LUMIFLON® and from Daikin Industries under the trade name ZEFFLE®.
  • the fluoropolymer can include or be modified to include at least one reactive functional group.
  • a "reactive functional group” refers to an atom, group of atoms, functionality, or group having sufficient reactivity to form at least one covalent bond with another reactive group in a chemical reaction.
  • Non-limiting examples of reactive functional groups that can be used with the fluoropolymer include hydroxyl groups, thiol groups, (meth)acrylate groups, carboxylic acid groups, amine groups, epoxide groups, carbamate groups, amide groups, urea groups, isocyanate groups (including blocked isocyanate groups), and combinations thereof.
  • the fluoropolymer can comprise a hydroxyl value of less 300 mg KOH/g, less than 250 mg KOH/g, less than 200 mg KOH/g, less than 150 mg KOH/g, less than 100 mg KOH/g, or less than 50 mg KOH/g.
  • the fluoropolymer can also comprise a hydroxyl value of at least 1 mg KOH/g, or at least 10 mg KOH/g, or at least 20 mg KOH/g.
  • the hydroxyl value of the polyester polyol is determined by esterification of the sample with excess acetic anhydride.
  • the excess acetic anhydride is converted to acetic acid by hydrolysis and titrated potentiometrically with standard potassium hydroxide.
  • the volume difference of titrate potassium hydroxide between a blank (no reaction) and the sample corresponds to the acid content of the sample, from which the hydroxyl number is calculated as the number of milligrams of potassium hydroxide needed to neutralize the acid in one gram of sample.
  • the hydrolyzing solution used in the determination is a mixture of dimethylformamide, pyridine, and distilled water
  • the acetylating reagent is a mixture of acetic anhydride and dichloroethane with p- toluene sulphonic acid as the catalyst.
  • the fluoropolymer used with the coating compositions of the present invention can comprise at least 1 weight %, at least 5 weight %, at least 10 weight %, at least 20 weight %, 30 weight %, at least 40 weight %, at least 50 weight %, or at least 60 weight %, based on the total resin solids of the coating composition, which is the total solids of the fluoropolymer and any additional film forming resin and which does not include the crosslinker.
  • the fluoropolymer used with the coating compositions of the present invention can comprise up to 95 weight %, up to 90 weight %, up to 80 weight %, up to 70 weight %, or up to 60 weight %, based on the total resin solids of the coating composition.
  • the fluoropolymer can also comprise a range such as from 1 to 95 weight %, from 5 to 95 weight %, from 10 to 90 weight %, or from 20 to 80 weight %, from 40 to 90 weight %, or from 60 to 80 weight %, based on the rein solids of the coating composition.
  • the coating composition of the present invention also includes a polyester polyol.
  • the polyester polyol can comprise a reaction product obtained from a mixture of reactants including, but not limited to, an aliphatic diol, a polyol comprising 3 or more hydroxyl groups, and a cyclic polycarboxylic acid such as a cyclic diacid.
  • a "polyol” refers to a compound comprising two or more hydroxyl groups
  • a "diol” refers to a compound having only two hydroxyl groups.
  • the term “aliphatic” refers to non-aromatic straight, branched, or cyclic hydrocarbon structures that contain saturated carbon bonds.
  • the saturated carbon chain or chains of the aliphatic structures can also comprise and be interrupted by other elements including, but not limited to, oxygen, nitrogen, carbonyl groups, and combinations thereof.
  • the saturated carbon chain of the aliphatic structures can comprise, but is not limited to, ether groups, ester groups, and combinations thereof.
  • linear refers to a compound having a straight hydrocarbon chain
  • branched refers to a compound having a hydrocarbon chain with a hydrogen replaced by a substituent such as an alkyl group that branches or extends out from a straight chain
  • cyclic refers to a closed ring structure.
  • the aliphatic diol used to prepare the polyester polyol can comprise one or more aliphatic diols, such as at least two, at least three, or at least four aliphatic diols.
  • the mixture of reactants used to prepare the polyester polyol can comprise two different aliphatic diols.
  • the aliphatic diols can be linear, branched, and/or cyclic.
  • the mixture of reactants used to prepare the polyester polyol can include one or more, such as at least two, branched aliphatic diols that comprise at least 50 mole %, at least 60 mole %, at least 70 mole %, at least 80 mole %, at least 90 mole %, or at least 95 mole % of the total amount of diols used to prepare the polyester polyol.
  • the mixture of reactants used to prepare the polyester polyol can include one or more, such as at least two, branched aliphatic diols that comprise up to 98 mole % or up to 100 mole % of the total amount of diols used to prepare the polyester polyol. It is appreciated that the reactants can be free of certain aliphatic diols, such as cyclic aliphatic diols for example.
  • the aliphatic diols can include various types of diols including aliphatic ester glycols for example.
  • suitable aliphatic diols include ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,3-propane diol, 2- methyl-l,3-propanediol, 1,4-butane diol, 1,5-pentanediol, 2,2,4-trimethyl 1,3- pentanediol, 2,4-di ethyl- 1,5-pentanediol, 1,6-hexane diol, 2-ethyl-l,3-hexanediol, neopentyl glycol, propylene glycol, tetraethylene glycol, pentaethylene glycol, hexaethylene glycol, heptaethylene glycol, octaethylene glycol, nonaethylene glycol, decaethylene
  • the aliphatic diol can comprise at least 10 weight %, at least 15 weight %, at least 20 weight %, or at least 25 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the aliphatic diol can comprise up to 60 weight %, up to 50 weight %, up to 40 weight %, or up to 35 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the aliphatic diol can also comprise a range such as from 10 weight % to 60 weight %, from 15 weight % to 40 weight %, or from 25 weight % to 35 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the polyol comprising 3 or more hydroxyl groups can include various types of polyols such as aliphatic, aromatic, linear, branched, and/or cyclic polyols comprising 3 or more hydroxyl groups.
  • suitable polyols comprising 3 or more hydroxyl groups include trimethylolpropane, trimethylolethane, 1,2,5-hexanetriol, polyether triols, di-trimethylol propane, pentaerythritol, di- pentaerythritol, trimethylol butane, glycerol, tris(2-hydroxyethyl) isocyanurate, and combinations thereof.
  • the polyol comprising 3 or more hydroxyl groups can comprise at least 3 weight %, at least 5 weight %, at least 10 weight %, at least 20 weight %, at least 25 weight %, or at least 30 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the polyol comprising 3 or more hydroxyl groups can comprise up to 45 weight %, or up to 40 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the polyol comprising 3 or more hydroxyl groups can also comprise a range such as from 3 to 45 weight %, or from 10 to 40 weight %, or from 20 to 40 weight %, or from 25 to 40 weight %, or from 30 to 40 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the polyester polyol is prepared with a polycarboxylic acid comprising a cyclic polycarboxylic acid.
  • a polycarboxylic acid refers to an organic compound with two or more carboxylic acid groups or an ester, such as the methyl ester or ethyl ester, or anhydride of the acid.
  • a cyclic polycarboxylic acid refers to a component comprising at least one closed ring structure, such as a carbocycle, with two or more carboxylic acid groups or the ester or anhydride of the acid.
  • the cyclic polycarboxylic acid can include aromatic cyclic polycarboxylic acids, aliphatic cyclic polycarboxylic acids, and combinations thereof.
  • aromatic cyclic polycarboxylic acids, or the anhydride or ester thereof include terephthalic acid, isophthalic acid, orthophthalic acid, phthalic anhydride, trimellitic acid, trimellitic anhydride, and combinations thereof.
  • Non-limiting examples of aliphatic non-aromatic cyclic polycarboxylic acids, or the anhydride or ester thereof, include 1,4- cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, decahydronaphthalene dicarboxylic acid, 1,3-cyclopentanedicarboxylic acid, 1,1- cyclopropanedicarboxylic acid, hexahydrophthalic acid, hexahydrophthalic anhydride, and combinations thereof.
  • the polyester polyol described above can also be prepared with additional acid components including, but not limited to, linear and branched polycarboxylic acid components including the anhydrides or esters thereof.
  • additional acid components include, but are not limited to, succinic acid, adipic acid, azelaic acid, sebacic acid, glutaric acid, and combinations thereof.
  • the cyclic polycarboxylic acid comprises greater than 10 mole % such as at least 40 mole %, at least 50 mole %, at least 60 mole %, at least 70 mole %, at least 80 mole %, at least 90 mole %, at least 95 mole %, or at least 98 mole % of the total carboxylic acids used to prepare the polyester polyol including the anhydride and esters of such carboxylic acids.
  • the cyclic polycarboxylic acid comprises 100 mole % of the total carboxylic acid components used to prepare the polyester polyol including the anhydride and esters of such carboxylic acid components.
  • the total amount of acid components used to prepare the polyester polyol can comprise at least 5 weight %, at least 10 weight %, at least 15 weight %, at least 20 weight %, at least 25 weight %, or at least 30 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the total amount of acid components can comprise up to 70 weight %, up to 60 weight %, up to 50 weight %, or up to 45 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the total amount of acid components can also comprise a range such as from 5 to 70 weight %, or from 20 to 60 weight %, or from 30 to 50 weight % of the total weight of the reactants used to prepare the polyester polyol.
  • the polyester polyol can also be prepared in the presence of catalysts.
  • the catalyst may be any catalyst known in the art to be useful for the formation of polyesters.
  • non-limiting catalysts include triphenyl phosphite, butyl stannoic acid, and combinations thereof.
  • the mixture of reactants used to prepare the polyester polyol can be mixed together to form a molar ratio of hydroxyl group equivalents to carboxylic acid group equivalents of 1.2:1 or greater, 1.3:1 or greater, 1.4:1 or greater, 1.5:1 or greater, 1.8:1 or greater, 2.0: 1 or greater, 2.5: 1 or greater, or 3.0: 1 or greater.
  • the reactants described above can be mixed together to form a molar ratio of hydroxyl equivalents to carboxylic acid group equivalents of up to 3.5 : 1.
  • the reactants described above can also be mixed together to form a molar ratio range of hydroxyl equivalents to carboxylic acid group equivalents such as from 1.2:1 to 3.5:1, or from 1.5:1 to 3.5:1 or from 1.8:1 to 3.0:1, or from 2.0:1 to 3.0:1.
  • the polyester polyol formed from the mixture of reactants can comprise a weight average molecular weight of less than 10,000 g/mol, less than 8,000 g/mol, less than 6,000 g/mol, or less than 5,000 g/mol.
  • the weight average molecular weight is determined with gel permeation chromatography relative to linear polystyrene standards of 800 to 900,000 Da with tetrahydrofuran as the eluent at a flow rate of 1 ml min-1 using a Waters 2695 separation module with a Waters 410 differential refractometer (RI detector) and two PLgel Mixed-C (300x7.5 mm) columns for separation.
  • the polyester polyol can also have a hydroxyl value of greater than 200 mg KOH/g, greater than 250 mg KOH/g, greater than 300 mg KOH/g, or at least 325 mg KOH/g, or at least 350 mg KOH/g, or at least 375 mg KOH/g, or at least 400 mg KOH/g, or at least 425 mg KOH/g, or at least 450 mg KOH/g, or at least 475 mg KOH/g, or at least 500 mg KOH/g, or at least 525 mg KOH/g. Further, the polyester polyol can include a hydroxyl value of up to and including 550 mg KOH/g.
  • the polyester polyol can also include a hydroxyl value range such as from 200 to 550 mg KOH/g, from 250 to 500 mg KOH/g, from 300 to 550 mg KOH/g, from 350 to 525 mg KOH/g, or from 400 to 525 mg KOH/g.
  • the hydroxyl value is determined by esterification of the sample with excess acetic anhydride as previously described.
  • the polyester polyol and, optionally, any of the additional components that make up the coating composition described herein can be substantially free, essentially free, or completely free of polymerizable ethylenically unsaturated groups.
  • substantially free as used in this context means the polyester polyol and, optionally, any of the additional components that make up the coating composition contain less than 1000 parts per million (ppm), "essentially free” means less than 100 ppm, and “completely free” means less than 20 parts per billion (ppb) of polymerizable ethylenically unsaturated groups based on the total weight of the polyester polyol and, optionally, any of the additional components that make up the coating composition described herein.
  • ppm parts per million
  • essentially free means less than 100 ppm
  • completely free means less than 20 parts per billion (ppb) of polymerizable ethylenically unsaturated groups based on the total weight of the polyester polyol and, optionally, any of the additional components that make up the coating composition described herein
  • ethylenically unsaturated refers to a group having at least one carbon-carbon double bond.
  • polymerizable ethylenically unsaturated refers to an ethylenically unsaturated group that participates in chemical reactions.
  • the polyester polyol can comprise at least 5 weight %, at least 10 weight %, at least 15 weight %, or at least 20 weight % of the coating composition, based on the total resin solids weight of the coating composition, which is the total solids of the fluoropolymer, polyester polyol, and optional additional film-forming resins and which does not include the crosslinker.
  • the polyester polyol can comprise up to 99 weight %, up to 90 weight %, up to 80 weight %, up to 70 weight %, up to 60 weight %, up to 50 weight %, or up to 40 weight % of the coating composition, based on the total resin solids of the coating composition.
  • the polyester polyol can also comprise a range such as from 5 to 99 weight %, from 10 to 60 weight %, or from 20 to 40 weight % of the coating composition, based on the total resin solids of the coating composition.
  • the coating composition also comprises a crosslinker that is reactive with at least the functional groups of the fluoropolymer and the polyester polyol.
  • a crosslinker refers to a molecule comprising two or more functional groups that are reactive with other functional groups and which is capable of linking two or more monomers or polymer molecules through chemical bonds. It will be appreciated that the coatings of the present invention can cure through the reaction between the functional groups of the fluoropolymer and the polyester polyol, and the functional groups of the crosslinkers to form the resinous binder. “Curing” refers to bond formation resulting in the formation of a crosslinked coating. Curing may occur upon application of an external stimulus including, but not limited to, heat.
  • Non-limiting examples of crosslinkers include phenolic compounds, epoxy compounds, beta-hydroxy (alkyl) amide resins, alkylated carbamate resins, isocyanates, polyacids, anhydrides, organometallic acid-functional materials, polyamines, polyamides, aminoplasts, and mixtures thereof.
  • the crosslinkers can comprise, but are not limited to, compounds comprising isocyanate groups including blocked isocyanate groups, epoxide groups, acids groups, anhydride groups, amino groups such as primary and secondary amino groups, amide groups, aminoplast based compounds, and combinations thereof.
  • Non-limiting examples of isocyanates include multifunctional isocyanates (polyisocyanates) such as linear, branched, and/or cyclic polyisocyanates.
  • the polyisocyanates can also be selected to only include certain types of polyisocyanates such as only linear and branched non-cyclic polyisocyanates for example.
  • multifunctional polyisocyanates include aliphatic diisocyanates such as hexamethylene diisocyanate and isophorone diisocyanate, and aromatic diisocyanates such as toluene diisocyanate and 4,4'-diphenylmethane diisocyanate.
  • the polyisocyanates can be blocked or unblocked.
  • polyisocyanates examples include isocyanurate trimers, allophanates, and uretdiones of diisocyanates and polycarbodiimides such as those disclosed in U.S. Patent No. 8,389,113 at column 4, lines 10-40, which is incorporated by reference herein.
  • the polyisocyanates can also be selected from polyisocyanates that do not include (i.e., are free of) isocyanurate trimers, allophanates, or uretdiones.
  • Suitable polyisocyanates are well known in the art and widely available commercially. Examples of commercially available isocyanates include DESMODUR® N 3300A, DESMODUR® Z 4470BA, DESMODUR® N 3900, and DESMODUR® N 3400, which are commercially available from Bayer Corporation.
  • Non-limiting examples of aminoplasts include condensates of amines and/or amides with aldehyde.
  • the most common amines or amides are melamine, urea, or benzoguanamine.
  • the condensate of melamine with formaldehyde is a suitable aminoplast.
  • condensates with other amines or amides can be used; for example, aldehyde condensates of glycoluril. While the aldehyde used is most often formaldehyde, other aldehydes such as acetaldehyde, crotonaldehyde, and benzaldehyde may be used.
  • the aminoplast contains methylol groups and at least a portion of these groups may be etherified with an alcohol to modify the cure response.
  • Any monohydric alcohol may be employed for this purpose including methanol, ethanol, butanol, and hexanol.
  • Non-limiting examples of commercially available aminoplasts that can be used include CYMEL® 303, CYMEL® 322, CYMEL® 327, CYMEL® 380, and CYMEL® 1130 (available from Cytec Industries and/or Allnex).
  • the crosslinker can also be added to the coating composition such that an equivalent ratio of the reactive functional groups on the crosslinker to reactive functional groups on the fluoropolymer and the polyester polyol is from 0.75:1 to 1.5:1, from 0.90:1 to 1.4:1, or from 1.05:1 to 1.25:1.
  • the crosslinker can comprise isocyanate groups and the fluoropolymer and the polyester polyol can comprise hydroxyl groups such that a ratio of total isocyanate equivalents to total hydroxyl equivalents is from 0.75:1 to 1.5:1, from 0.90:1 to 1.4:1, or from 1.05:1 to 1.25:1.
  • the coating composition can also include particles to further adjust the properties of coatings formed from the compositions of the present invention.
  • particles can be added to: lower gloss; improve abrasion, rub, and/or scratch resistance; control viscosity; and/or enhance soft touch properties such as the film hardness, coefficient of friction, and surface roughness.
  • the particles can be inorganic and/or organic particles.
  • suitable particles include metal hydroxides, metal oxides, silicas, pyrogenic silica, wax -treated silica, micronized wax, polyether condensate, polyamide microbeads, polyurethane microbeads, silicone microbeads, and combinations thereof.
  • micronized waxes include polytetrafluoroethylene wax, polytetrafluoroethylene-modified polyethylene wax, polytetrafluoroethylene-modified polypropylene wax, carnauba wax, silicone wax, polyethylene wax, polypropylene wax, paraffinic wax, and combinations thereof.
  • the particles added to the coating compositions can have an average particle size of at least 0.5 micron, at least 1 micron, or at least 1.5 microns.
  • the particles can have an average particle size of up to 30 microns, up to 25 microns, or up to 20 microns.
  • the particles can also have an average particle size range such as from 0.5 micron to 30 microns, 0.5 micron to 20 microns, or from 1 micron to 20 microns.
  • average particle size refers to the mean (average) particle size of the total amount of particles in a sample as determined by laser diffraction analysis.
  • the average particle size can be determined by a Malvern Mastersizer 2000 particle size analyzer following the instructions described in the Mastersizer 2000 manual.
  • soft touch coatings refer to coatings that can impart a range of soft touch or feel, for example, a velvety touch or feel, a silky touch or feel, or a rubbery touch or feel, to a substrate.
  • the particles can be added such that a weight ratio of the particles to the total amount of the fluoropolymer, the polyester polyol, and crosslinker (i.e., the binder of the coating composition) is at least 0.05:1, at least 0.10:1, or at least 0.12:1.
  • the particles can be added such that a weight ratio of the particles to the total amount of the fluoropolymer, polyester polyol, and crosslinker (collectively, the binder), referred to as particles to binder ratio, is at most 0.25:1, at most 0.20:1, or at most 0.15:1.
  • the particles can also be added such that a weight ratio range of the particles to the total amount of the fluoropolymer, polyester polyol, and crosslinker is from 0.05:1 to 0.25:1, from 0.05:1 to 0.20:1, or from 0.10:1 to 0.20:1.
  • the particles can comprise at least 0.5 weight %, at least 1 weight %, or at least 5 weight % of the coating composition, based on the total solid weight of the coating composition.
  • the particles can comprise up to 25 weight %, up to 20 weight %, or up to 15 weight % of the coating composition, based on the total solid weight of the coating composition.
  • the particles can also comprise a range such as from 0.5 to 25 weight %, from 1 to 20 weight %, or from 5 to 15 weight % of the coating composition, based on the total solid weight of the coating composition.
  • the coating compositions can further include a silicone component.
  • a "silicone component” refers to a component such as a polymer in which at least a portion of its chemical structure comprises alternate silicon and oxygen atoms.
  • the silicone component can comprise at least one, at least two, or at least three reactive functional groups that are reactive with at least the crosslinker.
  • the reactive functional groups can include, but are not limited to, a hydroxyl group, thiol group, (meth)acrylate group, carboxylic acid group, amine group, epoxide group, carbamate group, amide group, urea group, isocyanate group (including blocked isocyanate group), and combinations thereof.
  • the reactive functional groups can be bonded directly to a silicon atom.
  • the silicone component can include polymers with side chains comprising alternating silicon and oxygen atoms and which may include any of the reactive functional groups previously described.
  • the silicone component can comprise a silicone-modified polymer including, but not limited to, (meth)acrylate polymers, polyether polymers, polyamide polymers, polyamine polymers, and combinations thereof, and which include side chains that extend out from the backbone or main chain of such polymers and comprise alternate silicon and oxygen atoms.
  • the reactive functional groups can be bonded directly to a silicon atom.
  • a non-limiting example of such a silicone component is a hydroxyl-functional silicone-modified polyacrylate such as BYK®-SILCLEAN 3700 available from Byk Additives & Instruments.
  • suitable silicone components include polyalkylsiloxanes and which may include any of the reactive functional pendant and/or terminal groups previously described.
  • the silicone components can include, but are not limited to, polymethylsiloxanes, polydimethylsiloxanes, and combinations thereof and which may include any of the reactive functional pendant and/or terminal groups.
  • the silicone component can comprise at least 0.05 weight %, at least 0.1 weight %, at least 0.2 weight %, or at least 1 weight % of the coating composition, based on the total solid weight of the coating composition, i.e. all solid components used.
  • the silicone component can comprise up to 10 weight %, up to 8 weight %, or up to 5 weight % of the coating composition, based on the total solid weight of the coating composition.
  • the silicone component can also comprise a range such as from 0.05 to 10 weight % or from 0.2 to 5 weight % of the coating composition, based on the total solid weight of the coating composition.
  • the coating compositions of the present invention can also include other optional materials.
  • the coating compositions can also comprise a colorant.
  • colorant refers to any substance that imparts color and/or other opacity and/or other visual effect to the composition.
  • the colorant can be added to the coating in any suitable form, such as discrete particles, dispersions, solutions, and/or flakes. A single colorant or a mixture of two or more colorants can be used in the coatings of the present invention.
  • Example colorants include pigments (organic or inorganic), dyes and tints, such as those used in the paint industry and/or listed in the Dry Color Manufacturers Association (DCMA), as well as special effect compositions.
  • a colorant may include, for example, a finely divided solid powder that is insoluble, but wettable, under the conditions of use.
  • a colorant can be organic or inorganic and can be agglomerated or non-agglomerated. Colorants can be incorporated into the coatings by use of a grind vehicle, such as an acrylic grind vehicle, the use of which will be familiar to one skilled in the art.
  • Example pigments and/or pigment compositions include, but are not limited to, carbazole dioxazine crude pigment, azo, monoazo, diazo, naphthol AS, salt type (flakes), benzimidazolone, isoindolinone, isoindoline and polycyclic phthalocyanine, quinacridone, perylene, perinone, diketopyrrolo pyrrole, thioindigo, anthraquinone, indanthrone, anthrapyrimidine, flavanthrone, pyranthrone, anthanthrone, dioxazine, triarylcarbonium, quinophthalone pigments, diketo pyrrolo pyrrole red (“DPPBO red”), titanium dioxide, carbon black, and mixtures thereof.
  • DPPBO red diketo pyrrolo pyrrole red
  • Example dyes include, but are not limited to, those that are solvent and/or aqueous based such as phthalo green or blue, iron oxide, bismuth vanadate, anthraquinone, and peryleneand quinacridone.
  • Example tints include, but are not limited to, pigments dispersed in water- based or water miscible carriers such as AQUA-CHEM 896 commercially available from Degussa, Inc., CHARISMA COLORANTS and MAXITONER INDUSTRIAL COLORANTS commercially available from Accurate Dispersions Division of Eastman Chemical, Inc.
  • AQUA-CHEM 896 commercially available from Degussa, Inc.
  • CHARISMA COLORANTS and MAXITONER INDUSTRIAL COLORANTS commercially available from Accurate Dispersions Division of Eastman Chemical, Inc.
  • Non-limiting examples of materials that can be used with the coating compositions of the present invention include plasticizers, abrasion resistant particles, corrosion resistant particles, corrosion inhibiting additives, fillers including, but not limited to, micas, talc, clays, and inorganic minerals, anti-oxidants, hindered amine light stabilizers, UV light absorbers and stabilizers, surfactants, flow and surface control agents, thixotropic agents, organic solvents, organic cosolvents, reactive diluents, catalysts, reaction inhibitors, and other customary auxiliaries.
  • plasticizers including, but not limited to, micas, talc, clays, and inorganic minerals, anti-oxidants, hindered amine light stabilizers, UV light absorbers and stabilizers, surfactants, flow and surface control agents, thixotropic agents, organic solvents, organic cosolvents, reactive diluents, catalysts, reaction inhibitors, and other customary auxiliaries.
  • Non-limiting examples of suitable organic solvents include polar organic solvents e.g. protic organic solvents such as glycols, glycol ether alcohols, alcohols; and ketones, glycol diethers, esters, and diesters.
  • polar organic solvents e.g. protic organic solvents such as glycols, glycol ether alcohols, alcohols; and ketones, glycol diethers, esters, and diesters.
  • the coatings formed from the coating compositions of the present invention can be applied to a wide range of substrates known in the coatings industry.
  • the coatings of the present invention can be applied to automotive substrates including automotive interior substrates such as dashboards, industrial substrates, packaging substrates, wood flooring and furniture, apparel, electronics, including housings and circuit boards, glass and transparencies, sports equipment, including golf balls, and the like.
  • automotive substrates including automotive interior substrates such as dashboards, industrial substrates, packaging substrates, wood flooring and furniture, apparel, electronics, including housings and circuit boards, glass and transparencies, sports equipment, including golf balls, and the like.
  • These substrates can be, for example, metallic or non-metallic.
  • Metallic substrates include, but are not limited to, tin, steel (including electrogalvanized steel, cold rolled steel, hot-dipped galvanized steel, among others), aluminum, aluminum alloys, zinc-aluminum alloys, steel coated with a zinc-aluminum alloy, and aluminum plated steel.
  • Non-metallic substrates include polymeric, plastic, polyester, polyolefin, polyamide, cellulosic, polystyrene, polyacrylic, poly(ethylene naphthalate), polypropylene, polyethylene, nylon, EVOH, polylactic acid, other "green” polymeric substrates, poly(ethyleneterephthalate) (PET), polycarbonate, polycarbonate acrylonitrile butadiene styrene (PC/ABS), polyamide, wood, veneer, wood composite, particle board, medium density fiberboard, cement, stone, glass, paper, cardboard, textiles, leather, both synthetic and natural, and the like.
  • PET poly(ethyleneterephthalate)
  • PC/ABS polycarbonate acrylonitrile butadiene styrene
  • the coatings of the present invention are particularly useful when applied to automotive interiors and consumer electronic products.
  • the coatings of the present invention can be applied to substrates found on laptops, tablets, cellular phones, other handheld electronic devices, and the like.
  • the present invention further includes an electronic device or electronic component having a surface at least partially coated with the coating compositions described herein.
  • electronic device and like terms refers to any kind of device capable of processing data which is transmitted or received to or from any external entity.
  • An “electronic component” refers to a component associated with or part of an electronic device.
  • the coatings formed from the coating compositions of the present invention can be applied by any means standard in the art, such as electrocoating, spraying, electrostatic spraying, dipping, rolling, brushing, and the like.
  • the coatings of the present invention can be applied to a dry film thickness of 10 ⁇ to 100 ⁇ , 12 ⁇ to 70 ⁇ , or 15 ⁇ to 45 ⁇ .
  • the coating compositions of the present invention may also be used alone or in combination with primers and/or basecoats.
  • a "primer coating composition” refers to a coating composition from which an undercoating may be deposited onto a substrate in order to prepare the surface for application of a protective or decorative coating system.
  • a basecoat refers to a coating composition from which a coating is deposited onto a primer and/or directly onto a substrate optionally including components (such as pigments) that impact the color and/or provide other visual impact and which may be overcoated with a protective and decorative coating system.
  • the coating compositions can be applied to a substrate and cured to form coatings that have good stain resistance.
  • coatings formed from the coating compositions described herein have been found to exhibit a Delta E (DE or ⁇ ) of less than 20, less than 15, less than 12, less than 10, less than 8, less than 6, less than 4, less than 2, or less than 1 for mustard and lipstick stains after at least 168 hours of exposure.
  • coatings formed from the coating compositions described herein have also been found to exhibit a Delta E (DE or ⁇ ) of less than 3, less than 2, or less than 1 for sun screen, hand lotion, coffee, ketchup, stamp ink, cola, and sebum stains after at least 168 hours of exposure.
  • the Delta E (DE or ⁇ ) values were determined by a GretagMacBeth Color-Eye® 2145 Spectrophotometer with a cool white fluorescent light source.
  • the DE value is based on the CIE94 color system using L*a*b* coordinates, and, as used herein, refers to the difference between the color of unstained and stained coating samples.
  • the DE value is measured using the following method: (1) apply a coating to a substrate using a coating composition described herein; (2) measure the color of the unstained coated substrate; (3) apply a substance such as those described above to induce staining on the coating; (4) after a certain period of time, such as 168 hours of exposure, gently wipe the staining substance off of the coated sample with isopropanol or a soap solution; and (5) calculate the DE value from the color change between the unstained coating and the stained coating. The lower the DE value exhibited by the coating, the greater the stain resistance provided by the coating.
  • the described method is also referred to as the "staining test method.”
  • the coating compositions can be applied to a substrate and cured to form coatings that have a soft, smooth touch or feel.
  • coatings formed from the coating compositions described herein have been found to exhibit: a Fischer microhardness of less than 180 N/mm 2 , or less than 160 N/mm 2 , or less than 140 N/mm 2 , as measured by a Fischerscope FDVI2000 stylus microhardness instrument following the instruction described in the Fischerscope FDVI2000 Manual ("Fischer microhardness test"); a coefficient of friction ranging from 0.01 to 0.50, or from 0.05 to 0.4, or from 0.1 to 0.3, as measured by a Dynisco Polymer Test - 1055 coefficient of friction tester utilizing a felt contact according to ASTM Method D1894-14; and/or a surface roughness of 1 micro-inch to 60 micro-inches, or 5 micro-inch to 60 micro-inches, or from 8 micro-inches to 40 micro-inches, or from 10 micro-inches
  • “Fischer microhardness” refers to the hardness of a material to deformation
  • coefficient of friction refers to the ratio of the force that maintains contact between an object and a surface and the frictional force that resists the motion of the object
  • surface roughness refers to the texture of a surface such as the texture of a surface of a coating that is quantified by the vertical deviations of the surface from its ideal form.
  • a fluoro -ethylene alkyl-vinyl ether copolymer having hydro xyl functionality A fluoro -ethylene alkyl-vinyl ether copolymer having hydro xyl functionality.
  • each of the coating compositions listed in Table 3 were prepared by mixing methyl n-amyl ketone, xylene, acetone, polyester polyol resin, fluoropolymer resin, DISPERBYK®-2163, and BYK®-322 in an un-lined paint can at ambient temperature using an appropriately sized Cowles blade. Once the components formed a homogenous solution, SYLOID® CP4-8991 was slowly added to the solution. The speed of the Cowles blade was then increased and the mixture was allowed to grind for 30 minutes. After grinding, 10% dibutyltin dilaurate in n-butyl acetate, BYK®-SILCLEAN 3700, and Desmodur® N 3300 were added to the solution.
  • Example 2-5 The coating compositions of Examples 2-5 were sprayed onto a white colored polycarbonate/acrylonitrile butadiene styrene (PC/ABS) substrate.
  • PC/ABS polycarbonate/acrylonitrile butadiene styrene
  • the coated panels were allowed to flash off excess solvent for 5 minutes at ambient temperature before being placed in a heated oven at 60°C for 30 minutes. After the initial 30 minutes, the panels were post cured for 8 hours at 80°C.
  • the coatings had a dry film thickness of 25-35 microns.
  • each of the coatings formed from the compositions of Examples 2-5 were evaluated for stain resistance.
  • Example 5 As shown in Table 5, the coatings formed from the compositions of Examples 2-5 all exhibited a 60° gloss of 5 to 6. Further, Example 2 exhibited the best stain resistant followed by Examples, 3, 4, and 5, respectively. The coating of Example 5 exhibited lower stain resistance with higher DE values than the coatings of Examples 2-4. Referring to Tables 1-3, Example 5 was prepared with a polyester polyol having a hydroxyl value of 251 mg KOH/g, while Examples 2, 3, and 4 were prepared with polyester polyols having a hydroxyl value of 501 mg KOH/g, 402 mg KOH/g, and 310 mg KOH/g, respectively.
  • Glycol ether solvent commercially available from The Dow Chemical Company.
  • the coating compositions of Examples listed in Table 6 were prepared by mixing DOWANOLTM PM Acetate, methyl isobutyl ketone, methyl n-amyl ketone, xylene, polyester polyol resin, fluoropolymer resin, DISPERBYK®-2163, and BYK®- 322 in an un-lined paint can at ambient temperature using an appropriately sized Cowles blade. Once the components formed a homogenous solution, SYLOID® CP4-8991 was slowly added to the solution. The speed of the Cowles blade was then increased and the mixture was allowed to grind for 30 minutes.
  • Example 6-9 The coating compositions of Examples 6-9 were sprayed onto a white colored polycarbonate/acrylonitrile butadiene styrene (PC/ABS) substrate.
  • PC/ABS polycarbonate/acrylonitrile butadiene styrene
  • the coated panels were allowed to flash off excess solvent for 5 minutes at ambient temperature before being placed in a heated oven at 60°C for 30 minutes. After the initial 30 minutes, the panels were post cured for 8 hours at 80°C.
  • the coatings had a dry film thickness of 25-35 microns.
  • Heinz® Tomato Ketchup commercially available from H.J. Heinz Company.
  • Synthetic Sebum commercially available from Scientific Services S/D Inc.
  • Example 9 which comprised a polyester polyol prepared with an aliphatic cyclic polycarboxylic acid, exhibited better stain resistance than Comparative Examples 6, 7, and 8, which comprised a polyester polyol prepared with a linear polycarboxylic acid.
  • the coating compositions of Examples 10 and 11 listed in Table 9 were prepared by mixing methyl n-amyl ketone, xylene, acetone, polyester polyol resin, fluoropolymer resin, DISPERBYK®-2163, and BYK®-322 in an un-lined paint can at ambient temperature using an appropriately sized Cowles blade. Once the components formed a homogenous solution, SYLOID® CP4-8991 was slowly added to the solution. The speed of the Cowles blade was then increased and the mixture was allowed to grind for 30 minutes.
  • Example 10-11 The coating compositions of Examples 10-11 were sprayed onto a white colored polycarbonate/acrylonitrile butadiene styrene (PC/ABS) substrate.
  • PC/ABS polycarbonate/acrylonitrile butadiene styrene
  • the coated panels were allowed to flash off excess solvent for 5 minutes at ambient temperature before being placed in a heated oven at 60°C for 30 minutes. After the initial 30 minutes, the panels were post cured for 8 hours at 80°C.
  • the coatings had a dry film thickness of 25-35 microns.
  • Example 11 As shown in Table 11, the coatings formed from the compositions of Examples 10-11 exhibited a 60° gloss of 7 to 8. Further, Example 11, which comprised a polyester polyol prepared with an ester diol, exhibited better stain resistance than Example 10, which comprised a polyester polyol prepared with a non-ester diol.
  • the coating compositions of Examples 12 and 13 were prepared by mixing methyl n-amyl ketone, xylene, acetone, polyester polyol resin, fluoropolymer resin, DISPERBYK®-2163, and BYK®-322 in an un-lined paint can at ambient temperature using an appropriately sized Cowles blade. Once the components formed a homogenous solution, SYLOID® CP4-8991 was slowly added to the solution. The speed of the Cowles blade was then increased and the mixture was allowed to grind for 30 minutes. After grinding, 10% dibutyltin dilaurate in n-butyl acetate, BYK®-SILCLEAN 3700, and Desmodur® N 3300 were added to the solution.
  • the coating solution was thinned with a 40:60 blend of MAK: acetone resulting in a viscosity of 10- 12 seconds when measured by a #2 Iwata cup.
  • Various properties of the coating compositions are listed in Table 13.
  • Example 12 and 13 were sprayed onto a white colored polycarbonate/acrylonitrile butadiene styrene (PC/ABS) substrate.
  • PC/ABS polycarbonate/acrylonitrile butadiene styrene
  • the coated panels were allowed to flash off excess solvent for 5 minutes at ambient temperature before being placed in a heated oven at 60°C for 30 minutes. After the initial 30 minutes, the panels were post cured for 8 hours at 80°C.
  • the coatings had a dry film thickness of 25-35 microns.
  • Example 13 which comprised a polyester polyol prepared with an aromatic polycarboxylic acid, exhibited improved stain resistance as compared to Example 12, which comprised a polyester polyol prepared with an aliphatic cyclic polycarboxylic acid. It is noted that the polyester polyols in Examples 12 and 13 had similar hydroxyl values of around 500 mg KOH/g.
  • Example 9 As shown in Table 15, the coating formed from the composition of Example 9 exhibited good soft touch properties, i.e. a soft, smooth surface with low friction.
  • Two (2) different polyester polyol samples were prepared by independently mixing their respective components listed in Table 16 in a suitable reaction vessel. The contents of the vessel was heated to 140°C and a nitrogen cap was switched to a nitrogen sparge. Heating was continued to 180°C at which time water began to evolve from the reaction. The temperature of the reaction mixture was raised to 215°C in stages and held for a period of time. The contents of the reactor were cooled to less than 80°C and poured out. Various properties of each polyester polyol sample are shown in Table 17.
  • Tetrafluoroethylene based fluoropolymer commercially available from Daikin Industries, Inc.
  • the coating compositions of Examples 16-18 were prepared by mixing methyl n-amyl ketone, n-butyl acetate, acetone, polyester polyol resin, Zeffle® S-7530 , DISPERBYK®-2163, and BYK®-322 in an un-lined paint can at ambient temperature using an appropriately sized Cowles blade. Once the components formed a homogenous solution, SYLOID® CP4-8991 was slowly added to the solution. The speed of the Cowles blade was then increased and the mixture was allowed to grind for 30 minutes.
  • Example 16-18 The coating compositions of Examples 16-18 were sprayed onto a white colored polycarbonate/acrylonitrile butadiene styrene (PC/ABS) substrate.
  • PC/ABS polycarbonate/acrylonitrile butadiene styrene
  • the coated panels were allowed to flash off excess solvent for 5 minutes at ambient temperature before being placed in a heated oven at 60°C for 30 minutes. After the initial 30 minutes, the panels were post cured for 8 hours at 80°C.
  • the coatings had a dry film thickness of 25-35 microns.
  • Example 16 As shown in Table 19, the coatings formed from the compositions of Examples 16 and 17 exhibited a 60° gloss of about 3 while the coating formed from the composition of Example 18 exhibited a 60° gloss of 7. Further, Example 17 exhibited better stain resistance than Example 16, which comprised a polyester polyol prepared with a lower amount of trimethylol propane than the polyester polyol used in Example 17.
  • Example 17 which was prepared with an aromatic cyclic polycarboxylic acid and which had a hydroxyl value of 246.19 mg KOH/g, exhibited good stain resistance when compared to the good stain resistance coating formed from the composition of Example 18, which was prepared with an aliphatic cyclic polycarboxylic acid and which had a hydroxyl value of 512 mg KOH/g.
  • One (1) coating composition was prepared from the components listed in Table 20.
  • Silicone-containing surface additive polyester-modified, with hydroxyl functionality, commercially available from The Dow Chemical Company.
  • Example 19 The coating composition of Example 19 was prepared by mixing DOWANOLTM PM Acetate, methyl isobutyl ketone, n-butyl acetate, polyester polyol resin, DISPERBYK®-2163, and BYK®-370 in an un-lined paint can at ambient temperature using an appropriately sized Cowles blade. Once the components formed a homogenous solution, SYLOID® CP4-8991 was slowly added to the solution. The speed of the Cowles blade was then increased and the mixture was allowed to grind for 30 minutes. After grinding, 10% dibutyltin dilaurate in n-butyl acetate, BYK®- SILCLEAN 3700, and DESMODUR® N 3300 were added to the solution.
  • the coating solution was thinned with a 40:60 blend of MAK:acetone resulting in a viscosity of 9-12 seconds when measured by a #2 Iwata cup.
  • Various properties of the coating compositions are listed in Table 21.
  • Comparative Example 19 The coating composition of Comparative Example 19 was sprayed onto a white colored polycarbonate/acrylonitrile butadiene styrene (PC/ABS) substrate.
  • PC/ABS polycarbonate/acrylonitrile butadiene styrene
  • the coated panels were allowed to flash off excess solvent for 5 minutes at ambient temperature before being placed in a heated oven at 60°C for 30 minutes. After the initial 30 minutes, the panels were post cured for 8 hours in 80°C.
  • the coatings had a dry film thickness of 25-35 microns.
  • Table 22 also includes the stain resistant results of Example 12 for comparative purposes.
  • Example 12 which comprised the polyester polyol of sample 1 and a fluoropolymer, exhibited better stain resistance than Comparative Example 19, which comprised the polyester polyol of sample 1 and which did not include a fluoropolymer.
  • Example 12 particularly exhibited a significantly better stain resistance to mustard. It is appreciated that Comparative Example 19
  • Example 19 and Example 12 were both prepared with the same polyester polyol of sample 1, which had a high hydroxyl value of 512 mg KOH/g.
  • a coating composition comprising: (a) a fluoropolymer comprising at least one reactive functional group; (b) a polyester polyol comprising a reaction product prepared from a mixture of reactants comprising an aliphatic diol, a polyol comprising 3 or more hydroxyl groups, and a cyclic polycarboxylic acid, or an anhydride or ester thereof; and (c) a crosslinker reactive with (a) and (b).
  • Clause 2 The coating composition of clause 1, wherein the cyclic polycarboxylic acid (iii) comprises at least 40 mole %, at least 50 mole %, at least 60 mole %, at least 70 mole %, at least 80 mole %, at least 90 mole %, at least 95 mole %, or at least 98 mole % of the total carboxylic acids used to prepare the polyester polyol
  • Clause 3 The coating composition of clauses 1 or 2, wherein the fluoropolymer (a) comprises a fluoroethylene/alkyl vinyl ether copolymer that comprises at least one reactive functional group.
  • Clause 4 The coating composition of any of clauses 1 to 3, wherein the at least one reactive functional group of the fluoropolymer (a) comprises a hydroxyl group.
  • Clause 5 The coating composition of any of clauses 1 to 4 comprising the fluoropolymer (a) in an amount of from 40 to 90 weight % such as from 60 to 80 weight % of the total amount of (a) and (b).
  • Clause 6 The coating composition of any of clauses 1 to 5, further comprising particles having an average particle size of up to 30 microns.
  • Clause 7 The coating composition of clause 6, wherein the particles have an average particle size of 0.5 micron to 30 microns.
  • Clause 8 The coating composition of any of clauses 6 or 7, wherein the particles are inorganic particles such as silicas, metal hydroxides, and metal oxides.
  • Clause 9 The coating composition of any of clauses 6 to 8, wherein the coating composition comprises a weight ratio of the particles to the total of (a), (b), and (c) of 0.05:1 to 0.25:1.
  • Clause 10 The coating composition of any of clauses claim 1 to 9, wherein the polyester polyol (b) comprises a hydroxyl value of greater than 300 mg KOH/g.
  • Clause 11 The coating composition of any of clause 10, wherein the polyester polyol (b) has a hydroxyl value of at least 400 mg KOH/g.
  • Clause 12 The coating composition of any of clauses 1 to 11, wherein the polyester polyol (b) is completely free of polymerizable ethylenically unsaturated groups.
  • Clause 13 The coating composition of any of clauses 1 to 12, wherein the polyol (ii) comprising 3 or more hydroxyl groups comprises at least 20 weight % of the mixture of reactants used to prepare the polyester polyol (b) based on the total weight of the reactants.
  • Clause 14 The coating composition of any of clauses 1 to 13, wherein the cyclic polycarboxylic acid (iii) comprises an aliphatic cyclic polycarboxylic acid.
  • Clause 15 The coating composition of any of clauses 1 to 13, wherein the cyclic polycarboxylic acid (iii) comprises an aromatic cyclic polycarboxylic acid.
  • Clause 16 The coating composition of any of clauses 1 to 15, wherein the molar ratio of hydroxyl group equivalents to carboxylic acid group equivalents of the reactants forming the polyester polyol (b) is from 1.2:1 to 3.5:1 such as from 1.8:1 to 3.0:1.
  • Clause 17 The coating composition of any of clauses 1 to 16, wherein the polyester polyol (b) is prepared with at least two different aliphatic diols (i).
  • Clause 18 The coating composition of any of clauses 1 to 17, wherein the aliphatic diol (i) comprises a branched aliphatic diol.
  • Clause 19 The coating composition of any of clauses 1 to 18, wherein the branched aliphatic diol (i) comprises 50 to 100 mol % such as 60 to 90 mol % of the total amount of diols to prepare the polyester poyol (b).
  • Clause 20 The coating composition of any of clauses 1 to 19, wherein the diol (i) comprises 3-hydroxy-2,2-dimethylpropyl 3-hydroxy-2,2-dimethylpropanoate.
  • Clause 21 The coating composition of any of clauses 1 to 20, wherein the polyester polyol (b) has a weight average molecular weight of less than 10,000 g/mol as determined by gel permeation chromatography versus a polystyrene standard relative to linear polystyrene standards of 800 to 900,000 Da with tetrahydrofuran as the eluent at a flow rate of 1 ml min-1 using a Waters 2695 separation module with a Waters 410 differential refractometer (RI detector) and two PLgel Mixed-C (300x7.5 mm) columns for separation.
  • RI detector Waters 410 differential refractometer
  • Clause 22 The coating composition of clause 21, wherein the polyester polyol (b) has a weight average molecular weight of less than 8,000 g/mol, less than 6,000 g/mol, or less than 5,000 g/mol, as determined by gel permeation chromatography versus a polystyrene standard relative to linear polystyrene standards of 800 to 900,000 Da with tetrahydrofuran as the eluent at a flow rate of 1 ml min-1 using a Waters 2695 separation module with a Waters 410 differential refractometer (RI detector) and two PLgel Mixed-C (300x7.5 mm) columns for separation.
  • RI detector Waters 410 differential refractometer
  • Clause 23 The coating composition of any of clauses 1 to 22, wherein the crosslinker (c) comprises a polyisocyanate.
  • Clause 24 The coating composition of any of clauses 1 to 23, wherein the molar ratio of reactive functional groups on the crosslinker (c) to reactive functional groups on components (a) and (b) is from 0.90:1 to 1.4:1 such as from 1.05:1 to 1.25:1.
  • Clause 25 The coating composition of any of clauses 1 to 24, further comprising a silicone component having at least one functional group that is reactive with the crosslinker.
  • Clause 26 The coating composition of clause 25, wherein the at least one reactive functional group of the silicone component is a hydroxyl group.
  • Clause 27 The coating composition of any of clause 25 or 26, wherein the silicone component comprises two or more reactive functional groups.
  • Clause 28 A substrate at least partially coated with a coating formed from the coating composition of any of clauses 1 to 27.
  • Clause 29 An electronic device or electronic component comprising a surface at least partially coated with a coating formed from the coating composition of any of clauses 1 to 27.
  • Clause 30 A method for coating a substrate such as an electronic device or electronic component, comprising applying the coating composition of any of clauses 1 to 27 and curing the coating composition.
  • Clause 31 Use of the coating composition of any of clauses 1 to 27 to coat an electronic device or electronic component.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Polyesters Or Polycarbonates (AREA)
EP16732824.4A 2015-06-09 2016-06-09 Fleckenbeständige soft-touch-beschichtungszusammensetzungen und daraus hergestellte beschichtungen Active EP3307802B2 (de)

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EP3307802B1 (de) 2019-11-06
PL3307802T3 (pl) 2020-05-18
EP3307802B2 (de) 2023-02-08
KR102122502B1 (ko) 2020-06-12
MX2017016073A (es) 2018-02-21
CN107690445B (zh) 2020-08-25
NZ738442A (en) 2018-09-28
AU2016274701B2 (en) 2018-11-15
CN107690445A (zh) 2018-02-13
WO2016201103A1 (en) 2016-12-15
AU2016274701A1 (en) 2018-01-18
US20180163072A1 (en) 2018-06-14
CA2988004A1 (en) 2016-12-15
KR20180016517A (ko) 2018-02-14
US10487232B2 (en) 2019-11-26
BR112017026515A2 (pt) 2018-08-14
TW201714906A (zh) 2017-05-01

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